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2-Methoxy-4-nitrobenzenesulfonyl chloride → HCID 47062662, 화합물

HRID 1186643
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HRID 1186643 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10]([NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[CH3:20])(=[O:12])=[O:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH3:21][O:22]C1C=C([N+]([O-])=O)C=CC=1S(Cl)(=O)=O>>[CH3:21][O:22][C:8]1[CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=[CH:6][C:7]=1[S:10]([NH:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH3:20])(=[O:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 3094582-Methoxy-4-nitrobenzenesulfonyl chlorideHCID 779038HCID 779038, 화합물

생성물 1

HCID 47062662HCID 47062662, 화합물수율 79%

실험 절차

(RK2-063-03)I This compound was prepared according to the procedure for compound 11a except using 2-methoxy-4 nitrobenzenesulfonyl chloride. Recrystallization from DCM/Hexanes obtained the required product as brown crystals (202 mg, 79%). Mp=127-129° C.; 1H NMR (400 MHz, CDCl3) δ 8.03 (d, J=8.8 Hz, 1H), 7.85-7.88 (m, 2H), 7.14-7.11 (m, 2H), 7.06-7.04 (m, 2H), 6.76 (br s, 1H), 4.13 (s, 3H), 2.26 (s, 3H).

후처리

  1. custom(RK2-063-03)I This compound was prepared
  2. customRecrystallization from DCM/Hexanes

출처 및 근거

ORD 기록
ord-8398755a411b44b8b279cd7fa4cb66a0
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08673910B2

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